A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088741



Internal ID20655781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5937292..5942578hg38UCSC Ensembl
chr2:6077424..6082710hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg385287
hg195287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353339
Supporting Variants
Samples
Known GenesLINC01105
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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